Pharmaceutical composition for piperidinoalkanol compounds

ABSTRACT

The invention provides a pharmaceutical composition in solid unit dosage form, comprising, a) a therapeutically effective amount of a piperidinoalkanol compound or a pharmaceutically acceptable salt thereof; and, b) at least one inert ingredient.

CROSS-REFERENCE TO RELATED APPLICATION

This is a division of application Ser. No. 08/552,287, filed Dec. 12,1995, now allowed, which is a continuation-in-part application Ser. No.08/395,952, filed Feb. 28, 1995, now abandoned, which are hereinincorporated by reference.

BACKGROUND OF THE INVENTION

It has been established that various piperidinoalkanol compounds areuseful as antihistamines, antiallergy agents and bronchodilators asdisclosed in U.S. Pat. Nos. 3,878,217, 4,254,129 and 4,285,957. Severalexamples of formulations of these various piperidinoalkanol compoundsare described below.

In U.S. Pat. No. 4,929,605, J. Domet and D. Shah describe apharmaceutical composition in solid unit dosage form, comprising, atherapeutically effective amount of a piperidinoalkanol compound, or apharmaceutically acceptable salt thereof, a pharmaceutically acceptablenonionic or cationic surfactant in an amount of from about 0.1% to about6% by weight of the composition, and a pharmaceutically acceptablecarbonate salt in an amount of from about 2% to about 50% by weight ofthe composition.

N. Webb and G. Hammer describe in U.S. Pat. No. 4,996,061, apharmaceutical composition in the form of a multiple-compression tabletcomprising a discrete zone made from a formulation which providessustained-release of a therapeutically effective decongestant amount ofa sympathomimetic drug and a discrete zone made from a differentformulation which provides immediate release of a therapeuticallyeffective antihistaminic amount of a piperidinoalkanol and, optionally,a therapeutically effective decongestant amount of a sympathomimeticdrug.

Efforts have focused on improving the bioavailability of variouspiperidinoalkanol compounds in order to improve their therapeuticefficiency. The present invention relates to pharmaceutical compositionsand pharmaceutical compositions in solid unit dosage form wherein thepiperidinoalkanol compound, or a pharmaceutically acceptable saltthereof, is in combination with inert ingredients.

SUMMARY OF THE INVENTION

The present invention provides a pharmaceutical composition in solidunit dosage form, comprising,

a) a therapeutically effective amount of a piperidinoalkanol compound ora pharmaceutically acceptable salt thereof; and

b) at least one inert ingredient.

The present invention further provides a pharmaceutical compositionprepared by a wet granulation process comprising, preparing the wetgranulation wherein a compound of the formula; ##STR1## wherein X is anumber ranging from about zero to 5, and the individual optical isomersthereof, a diluent and a disintegrant are mixed with a solution of abinding agent; the wet granulation is screened; and the wet granulationis dried. In addition, the present invention provides combining theabove dry granulation with a lubricant. The present invention furtherprovides pressing the above final mixture into a tablet.

DETAILED DESCRIPTION OF THE INVENTION

As used herein the terms "piperidinoalkanol compounds" and"piperidinoalkanol compounds and their pharmaceutically acceptablesalts" refers to those compounds described by formulas (I), (II) and(III) which are disclosed in U.S. Pat. Nos. 3,878,217, 4,254,129 and4,285,957 the disclosure of each patent being incorporated herein byreference. In addition, the patent application entitled "PharmaceuticalComposition Piperidinoalkanol Compounds', U.S. Ser. No. 08/395,952,filed Feb. 28, 1995 is incorporated herein by reference.

Piperidinoalkanol compounds of formula (I) are those which correspond tothe formula; ##STR2## wherein R₁ is hydrogen or hydroxy; R₂ is hydrogen;or R₁ and R₂ taken together form a second bond between the carbon atomsbearing R₁ and R₂ ; n is a positive whole integer of from 1 to 3; Z isthienyl, phenyl or substituted phenyl wherein the substituents on thesubstituted phenyl may be attached at the ortho, meta or para positionsof the unsubstituted phenyl ring and are selected from the groupconsisting of a halogen atom, a straight or branched lower alkyl chainof from 1 to 4 carbon atoms, a lower alkoxy group of from 1 to 4 carbonatoms, a di(lower)alkylamino group, or a saturated monocyclicheterocyclic ring selected from the group consisting of pyrolidino,piperidino, morpholino, or N-(lower)alkylpiperizino, or pharmaceuticallyacceptable acid addition salts thereof.

Piperidinoalkanol compounds of formula (II) are those which correspondto the formula; ##STR3## wherein R₁ represents hydrogen or hydroxy; R₂represents hydrogen; or R₁ and R₂ taken together form a second bondbetween the carbon atoms bearing R₁ and R_(2;) m is an integer of from 1to 5; R₃ is --CH₃ or --CH₂ OH; each A and B is hydrogen or hydroxy; withthe provisos that at least one of A or B is hydrogen and one of A or Bis other than hydrogen when R₃ is --CH_(3;) and pharmaceuticallyacceptable salts and individual optical isomers thereof.

Piperidinoalkanol compounds of formula (III) are those which correspondto the formula; ##STR4## wherein R₁ represents hydrogen or hydroxy; R₂represents hydrogen; or R₁ and R₂ taken together form a second bondbetween the carbon atoms bearing R₁ and R_(2;) m is an integer of from 1to 5; R₄ is --CO₂ H or --CO₂ alkyl wherein the alkyl moiety has from 1to 6 carbon atoms and is straight or branched; each of A and B ishydrogen or hydroxy; with the proviso that at least one of A or B ishydrogen; and pharmaceutically acceptable salts and individual opticalisomers thereof.

More specifically, 4- 4-4-(Hydroxydiphenylmethyl)-1-piperdinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride of formula (IIIa) ##STR5## wherein X is a numberranging from about zero to 5, and the individual optical isomersthereof, is a preferred piperidinoalkanol compound. The compound 4- 4-4-(Hydroxydiphenylmethyl)-1-piperdinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride wherein X is zero or one in formula (IIIa) is themost preferred piperidinoalkanol compound.

In addition, the free base of 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperdinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acid of formula(IIIb) ##STR6## wherein X is a number ranging from about zero to 5, andthe individual optical isomers thereof, is also a preferredpiperidinoalkanol compound.

Further included within the scope of the piperidinoalkanol compounds offormulas (III), (IIIa) and (IIIb) are the polymorphic, pseudomorphic andamorphous forms, and mixtures thereof. More specifically, the polymorphsof anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride which are designated herein as Form I and Form III.The Form I polymorph of anhydrous 4- 4- 4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride may be identified by the following characteristics: avisual melting point (capillary tube) in the range of about 196°-201°C.; a melt endotherm with extrapolated onset in the range of about195°-199° C. as determined by differential scanning calorimetry; and anX-ray powder diffraction pattern essentially as shown in Table 1 whereinthe XRPD patterns were measured using a powder diffractometer equippedwith a Co X-ray tube source. The sample was illuminated with Co Kα₁radiation and XRPD data were collected from 5° to 55° 2⊖. (intensitiesmay vary radically due to preferred orientation).

                  TABLE 1                                                         ______________________________________                                        D-Space, Angstroms                                                                            Intensity, I/I.sub.o, %                                       ______________________________________                                        11.8            30                                                            7.3             30                                                            6.3             65                                                            5.9             35                                                            5.0             45                                                            4.8             100                                                           4.4             45                                                            3.9             60                                                            3.8             75                                                            3.7             30                                                            ______________________________________                                    

The Form III polymorph of anhydrous 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride may be identified by the following characteristics: avisual melting point (capillary tube) in the range of about 166°-171°C.; a broad endotherm below about 90° C., a melt endotherm with anextrapolated onset of about 166° C. as determined by differentialscanning calorimetry; and an X-ray powder diffraction patternessentially as shown in Table 2 wherein the XRPD patterns were measuredusing a powder diffractometer equipped with a Co X-ray tube source. Thesample was illuminated with Co Kα₁ radiation and XRPD data werecollected from 5° to 55° 2⊖. (intensities may vary radically due topreferred orientation).

                  TABLE 2                                                         ______________________________________                                        D-Space, Angstroms                                                                            Intensity, I/I.sub.o, %                                       ______________________________________                                        9.0             95                                                            4.9             100                                                           4.8             35                                                            4.6             25                                                            4.5             25                                                            3.7             25                                                            ______________________________________                                    

In addition, the psuedomorphs of hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride are designated herein as Form II and Form IV. The Form IIpseudomorph of hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride may be identified by the following characteristics: avisual melting point (capillary tube) in the range, of about 100°-105°C.; a large broad endotherm below about 100° C. and a small endothermicpeak (about 2 joules/gram) with extrapolated onsets in the range ofabout 124°-126° C. as determined by differential scanning calorimetry;and an X-ray powder diffraction pattern essentially as shown in Table 3wherein the XRPD patterns were measured using a powder diffractometerequipped with a Co X-ray tube source. The sample was illuminated with CoKα₁ radiation and XRPD data were collected from 5° to 55 ° 2⊖.(intensities may vary radically due to preferred orientation).

                  TABLE 3                                                         ______________________________________                                        D-Space, Angstroms                                                                            Intensity, I/I.sub.o, %                                       ______________________________________                                        7.8             45                                                            6.4             44                                                            5.2             85                                                            4.9             60                                                            4.7             80                                                            4.4             55                                                            4.2             50                                                            4.1             60                                                            3.7             75                                                            3.6             60                                                            3.5             50                                                            ______________________________________                                    

The Form IV pseudomorph of hydrated 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride may be identified by the following characteristics: avisual melting point (capillary tube) in the range of about 113°-118°C.; two broad overlapping endotherms below about 100° C. and anadditional endotherm with an extrapolated onset at approximately 146° C.as determined by differential scanning calorimetry and an X-ray powderdiffraction pattern essentially as shown in Table 4 wherein the XRPDpatterns were measured using a powder diffractometer equipped with a CoX-ray tube source. The sample was illuminated with Co Kα₁ radiation andXRPD data were collected from 5° to 55° 2⊖. (intensities may varyradically due to preferred orientation).

                  TABLE 4                                                         ______________________________________                                        D-Space, Angstroms                                                                            Intensity, I/I.sub.o, %                                       ______________________________________                                        10.4            60                                                            7.0             45                                                            6.4             50                                                            5.3             100                                                           5.2             55                                                            4.3             75                                                            4.1             50                                                            4.0             45                                                            3.8             60                                                            3.5             55                                                            ______________________________________                                    

Included within the scope of the present invention are the pseudomorphsand polymorphs of the hydrated and anhydrous free base of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid. The free base of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid is readily prepared utilizing techniques and procedures well knownto one of ordinary skill in the art. For example, the hydrochloride saltof 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acid isdissolved in methanol and treated with one equivalent of aqueous sodiumbicarbonate. After stirring for approximately 5 to 30 minutes, the whitesolid is collected by filtration, rinsed with water and air dried toprovide the dihydrate of the free base of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acid.

Illustrative examples of straight or branched alkyl groups having from 1to 4 carbon atoms referred to herein are methyl, ethyl, n-propyl,isopropyl, n-bury, isobutyl and t-butyl. Illustrative examples ofstraight or branched alkyl groups having from 1 to 6 carbon atomsreferred to herein are methyl, ethyl, n-propyl, isopropyl, n-butyl,isobutyl, t-butyl, n-pentyl, cyclopentyl, n-hexyl and cyclohexyl.Illustrative examples of lower alkoxy groups of from 1 to 4 carbon atomsreferred to herein are methoxy, ethoxy, propoxy, n-butoxy, isobutoxy,sec-butoxy and t-butoxy. The terms "halo", "halogen" or "halide" refersto a fluorine, chlorine, bromine or iodine atom. The term"pharmaceutically acceptable salt" refers to those salts of formulas(I), (II), (III) and (IIIa) that are not substantially toxic at thedosage administered to achieve the desired effect and do notindependently possess significant pharmacological activity. The saltsincluded within the scope of this term are pharmaceutically acceptableacid addition salts of a suitable inorganic or organic acid. Suitableinorganic acids are, for example hydrochloric, hydrobromic, sulfuric andphosphoric acids. Suitable organic acids include carboxylic acids, suchas acetic, propionic, glycolic, lactic, pyruvic, malonic, succinic,fumaric, malic, tartaric, citric, cyclamic, ascorbic, maleic,hydroxymaleic, dihydroxymaleic, benzoic, phenylacetic, 4-aminobenzoic,4-hydroxybenzoic, anthranillic, cinnamic, salicylic, 4-aminosalicyclic,2-phenoxybenzoic, 2-acetoxybenzoic and mandelic acid, sulfonic acids,such as methanesulfonic, ethanesulfonic and β-hydroxyethanesulfonicacid. In addition, pharmaceutically acceptable salts include those saltsof formulas (I), (II), (III) and (IIIa) formed with inorganic andorganic bases, such as those of alkali metals, for example sodium,potassium and lithium, alkaline earth metals, for example calcium andmagnesium, light metals of group IIIA, for example aluminum, organicamines, for example primary, secondary or tertiary amines, such ascyclohexylamine, ethylamine, pyridine, methylaminoethanol andpiperazine. The salts are prepared by conventional means by one ofordinary skill in the art as, for example, by treating a compound offormulas (I), (II), (III) or (IIIa) with an appropriate acid or base.Such salts can exist in either a hydrated or substantially anhydrousform.

As used herein, the phrase "formulas I through IIIb" refers to formulasI, II, III, IIIa and IIIb.

As used herein, the term "azeotropic mixture" refers to a liquid mixtureof two or more substances which behaves like a single substance in thatthe vapor produced by partial evaporation of liquid has the samecomposition as the liquid. The constant boiling mixture exhibits eithera maximum or minimum boiling point as compared with that of othermixtures of the same substance.

As used herein, the term "azeotropic distillation" refers to a type ofdistillation in which a substance is added to the mixture to beseparated in order to form an azeotropic mixture with one or more of theconstituents of the original mixture. The azeotrope or azeotropes thusformed will have boiling points different from the boiling points of theoriginal mixture. As used herein, the term "azeotropic distillation"also refers to co-distillation.

As used herein, the term "water-minimizing recrystallization" refers toa recrystallization wherein the ratio of anhydrous solvent to substratehydrate is such that the percentage of water present is minimized,thereby inducing precipitation of the anhydrous form of the substrate.

As used herein, the term "aqueous recrystallization" refers to thoseprocesses wherein either 1) a solid material is dissolved in a volume ofwater or a water/organic solvent mixture sufficient to cause dissolutionand the solid material recovered by evaporation of the solvent; 2 asolid material is treated with a minimal amount of water or awater/organic solvent mixture which is not sufficient to causedissolution, heated to obtain dissolution and cooled to inducecrystallization or 3) a solid material is dissolved in a volume of wateror a water/organic solvent mixture sufficient to cause dissolution andthen the solvent is partially evaporated to form a saturated solutionwhich induces crystallization.

As used herein, the term "crystal digestion" refers to that processwherein a solid material is treated with a minimal amount of water orwater/organic solvent mixture which is not sufficient to causedissolution and either heating or stirring at ambient temperature untilthe desired transformation has taken place.

As used herein, the term "antisolvent" refers to a poor solvent for thesubstance in question which when added to a solution of the substance,causes the substance to precipitate.

As used herein, the term "suitable temperature" refers to thattemperature which is sufficient to cause dissolution and to permit theprecipitation of the desired substance either upon addition of anantisolvent or upon removal of the co-solvent by azeotropicdistillation.

The term "micronization" refers to the process of increasing theparticle surface area of the piperidinoalkanol compounds or theirpharmaceutically acceptable salts to greater than about 1.0 m² /g.

The piperidinoalkanol compounds of formulas (I) through (IlIb) which arenot subjected to micronization have a particle surface area of less thanabout 1.0 m² /g.

The pharmaceutical composition of the present invention is administeredorally in the form of a solid unit dosage form. Examples of solid unitdosage forms are tablets, coated tablets, powders, dragees, hard or softgelatin capsules and the like. The preferred solid unit dosage forms ofthe present invention are capsules, tablets and the like. The mostpreferred solid unit dosage form are tablets. A unit dose is that amountof the pharmaceutical composition which is individually administered.The pharmaceutical compositions of the present invention are useful asantihistamines, antiallergy agents, bronchodilators and in the treatmentof urticaria.

As used herein, the term "patient" refers to a warm-blooded animal, suchas a mammal, which is in need of an antihistamine, antiallergy agent,bronchodilator or treatment of urticaria. It is understood that humans,mice and rats are included within the scope of the term "patient".

A therapeutically effective amount can be readily determined by theattending diagnostician, as one skilled in the art, by the use of knowntechniques and by observing results obtained under analogouscircumstances. In determining the therapeutically effective amount ordose, a number of factors are considered by the attending diagnostician,including, but not limited to: the species of mammal; its size, age, andgeneral health; the response of the individual patient; the particularcompound administered; the mode of administration; the bioavailabilitycharacteristics of the preparation administered; the dose regimenselected; the use of concomitant medication; and other relevantcircumstances.

A therapeutically effective amount of a piperidinoalkanol compound offormulas (I) through (IIIb) is that amount which produces the desiredtherapeutic response (ie., antihistaminic, antiallergic, bronchodilatoryeffect, or reduction or elimination of urticaria) upon oraladministration according to a single or multiple dosage regimen. Atherapeutically effective amount of a piperidinoalkanol compound offormulas (I) through (IIIb) may vary over a wide range from about 0.01milligrams per kilogram (mg/kg) to about 20 (mg/kg) of body weight perdose. A pharmaceutical composition which provides from about 5 mg toabout 360 mg of a piperidinoalkanol compound of formulas (I) through(IIIb) per unit dose is preferred and those which provide from about 40mg to about 240 mg per unit dose are most preferred.

According to the present invention the piperidinoalkanol compounds offformulas (I) through (IIIb) when micronized have a particle surface areaof greater than about 1.0 m² /g. The preferred particle surface areawhen micronized is about 2 to 10 m² /g, the most preferred particlesurface area when micronized is about 2 to 6 m² /g and the mostespecially preferred particle surface area of the piperidinoalkanolcompounds of formulas (I) through (IIIb) when micronized is about 2 to 4m2/g.

The piperidinoalkanol compounds of formulas (I) through (IIIb) arereadily prepared by one of ordinary skill in the art, for example,utilizing the techniques and procedures described in U.S. Pat. Nos.3,878,217, 4,254,129 and 4,285,957, international Application NumberPCT/US93/02103 published Oct. 28, 1993, WO 93/21156, and internationalApplication Number PCT/US94/05982, published Jan. 5, 1995, WO 95/00480which are incorporated herein by reference.

The anhydrous, pharmaceutically acceptable acid addition salts of thepiperidinoalkanol compounds of the formulas (III), and (IIIa) may beprepared from the corresponding hydrated, pharmaceutically acceptableacid addition salts of the piperidinoalkanol compounds of the formulas(III) and (IIIa) by subjecting the corresponding hydrated,pharmaceutically acceptable acid addition salts of the piperidinoalkanolcompounds of the formulas (III) and (IIIa) to an azeotropicdistillation.

For example, the appropriate hydrated, pharmaceutically acceptable acidaddition salt of the piperidinoalkanol compounds of the formulas (III)and (IIIa) is first dissolved in a volume of a suitable solvent orsolvent mixture which is sufficient to cause dissolution. Examples ofsuch solvents are water, C_(1`-C) ₅ alkanols such as methanol, ethanoland the like; ketone solvents such as acetone, methyl ethyl ketone andthe like; aliphatic ester solvents such as ethyl acetate, methylacetate, methyl formate, ethyl formate, isopropyl acetate and the likeand aqueous mixtures of these solvents, such as acetone/water, methylethyl ketone/water, water/acetone and water/acetone/ethyl acetate. Anadditional volume of the same solvent used to effect dissolution orsecond suitable anhydrous antisolvent is then added to this solution,which is then heated to a boiling point which is suitable toazeotropically remove water and other low boiling components. Suitableanhydrous antisolvents for use in the azeotropic distillation are, forexample, ketone solvents such as acetone, methyl ethyl ketone and thelike; aliphatic ester solvents such as ethyl acetate, methyl acetate,methyl formate, ethyl formate, isopropyl acetate and the like; C₅ -C₈aliphatic solvents such as pentane, hexane and the like; aliphaticnitriles, such as acetonitrile and mixtures of these solvents such asacetone/ethyl acetate and the like. The azeotropic mixture of water andsolvent is removed by distillation until the temperature changes,indicating that the azeotropic mixture is completely removed. Thereaction mixture is cooled and the corresponding anhydrous,pharmaceutically acceptable acid addition salts of the piperidinoalkanolcompounds of the formulas (III) and (IIIa) is recovered from thereaction zone by, for example filtration.

In addition, the anhydrous, pharmaceutically acceptable acid additionsalts of the piperidinoalkanol compounds of the formulas (III) and IIIa)may be prepared from the corresponding hydrated, pharmaceuticallyacceptable acid addition salts of the piperidinoalkanol compounds of theformulas (III) and (IIIa) by subjecting the corresponding hydrated,pharmaceutically acceptable acid addition salts of the piperidinoalkanolcompounds of the formulas (III) and (IIIa) to a water-minimizingrecrystallization.

For example, the appropriate hydrated, pharmaceutically acceptable acidaddition salt of the piperidinoalkanol compounds of the formulas (III)and (IIIa) is dissolved in a volume of a suitable anhydrous solvent orsolvent mixture which is sufficient to cause dissolution and heated toreflux. Examples of such solvents are water, C₁ -C₅ alkanols such asmethanol, ethanol and the like; ketone solvents such as acetone, methylethyl ketone and the like; aliphatic ester solvents such as ethylacetate, methyl acetate, methyl formate, ethyl formate, isopropylacetate and the like and aqueous mixtures of these solvents, such asacetone/water, methyl ethyl ketone/water, water/acetone andwater/acetone/ethyl acetate. An additional volume of the same solventused to effect dissolution or second suitable anhydrous antisolvent isthen added in a quantity sufficient to initiate precipitation of theanhydrous, pharmaceutically acceptable acid addition salt of thepiperidinoalkanol compounds of the formulas (III) and (IIIa). Suitableanhydrous antisolvents are, for example, ketone solvents such asacetone, methyl ethyl ketone and the like; aliphatic ester solvents suchas ethyl acetate, methyl acetate, methyl formate, ethyl formate,isopropyl acetate and the like; mixtures of ketone solvents andaliphatic ester solvents such as acetone/ethyl acetate and the like; C₅-C₈ aliphatic solvents such as pentane, hexane and the like; aliphaticnitriles, such as acetonitrile and mixtures of these solvents such asacetone/ethyl acetate and the like as well as mixtures of water andketone solvents such as acetone/water and the like; and mixtures ofwater, ketone solvents and aliphatic ester solvents such asacetone/water/ethyl acetate. The reaction mixture is cooled and thecorresponding anhydrous, pharmaceutically acceptable acid addition saltof the piperidinoalkanol compounds of the formulas (III) and (IIIa) isrecovered from the reaction zone by, for example filtration.

Polymorphic forms of anhydrous 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Forms I and III) may be prepared by a variety of methodsas detailed below.

Form III to Form I

For example, anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form I) may be prepared from anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form III), by subjecting the anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form III) to a crystal digestion as described above.

Form II to Form III

In addition, anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form III) may be prepared from hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form II), by subjecting the hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form II) to water-minimizing recrystallization asdescribed above.

Form II to Form I

In addition, anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form I) may be prepared from hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form II), by subjecting the hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form II) to water-minimizing recrystallization asdescribed above or by subjecting the hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form II) to an azeotropic distillation.

Form IV to Form I

In addition, anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form I) may be prepared from hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form IV), by subjecting the hydrated 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form IV) to water-minimizing recrystallization or to anazeotropic distillation as described above.

The hydrated, pharmaceutically acceptable acid addition salts of thepiperidinoalkanol compounds of the formulas (III) and (IIIa) may beprepared from the corresponding compound of the formula (IV) ##STR7##wherein R₁ represents hydrogen or hydroxy; R₂ represents hydrogen; or R₁and R₂ taken together form a second bond between the carbon atomsbearing R₁ and R₂ m is an integer of from 1 to 5; R₄ is --CO₂ alkylwherein the alkyl moiety has from 1 to 6 carbon atoms and is straight orbranched; each of A and B is hydrogen or hydroxy; with the proviso thatat least one of A or B is hydrogen; by subjecting the correspondingcompound of formula (IV) to a reduction using an appropriate reducingagent, such as sodium borohydride, potassium borohydride, sodiumcyanoborohydride, or tetramethylammonium borohydride in a suitablesolvent, such as, methanol, ethanol, isopropyl alcohol or n-butanol,aqueous mixtures thereof or basic solutions thereof, at temperaturesranging from about 0° C. to the reflux temperature of the solvent, andthe reaction time varies from about 1/2hour to 8 hours. After quenchingand acidifying with an suitable acid, such as hydrochloric acid, thehydrated, pharmaceutically acceptable acid addition salts of thepiperidinoalkanol compounds of the formulas (III) and (IIIa) arerecovered from the reaction zone by crystallization and filtration.

In addition, the hydrated, pharmaceutically acceptable acid additionsalts of the piperidinoalkanol compounds of the formulas (III) and(IIIa) may be prepared from the corresponding anhydrous,pharmaceutically acceptable acid addition salts of the formulas (III),(IIIa) and (IIIb) by subjecting the corresponding anhydrous,pharmaceutically acceptable acid addition salts of formulas (III) and(IIIa) to an aqueous recrystallization.

For example, the appropriate anhydrous, pharmaceutically acceptable acidaddition salt of the piperidinoalkanol compounds of the formula (I) and(II) is treated with a minimal volume of water or suitable water/organicsolvent mixture which is insufficient to cause dissolution and heated toreflux. The reaction mixture is cooled and the corresponding hydrated,pharmaceutically acceptable acid addition salt of the piperidinoalkanolcompounds of the formulas (III) and (IIIa) is recovered from thereaction zone by, for example filtration. Alternatively, the appropriateanhydrous, pharmaceutically acceptable acid addition salt of thepiperidinoalkanol compounds of the formulas (III) and (IIIa) is treatedwith a volume of water or a suitable water/organic solvent mixture whichis sufficient to cause dissolution and the water or water/organicsolvent is partially or completely evaporated to a volume which inducescrystallization of the hydrated, pharmaceutically acceptable acidaddition salts of the piperidinoalkanol compounds of the formulas (III)and (IIIa). Suitable solvents for use in the above recrystallization arewater, acetone/water, ethanol/water, methyl ethyl ketone/aqueousmethanol, methyl ethyl ketone/water and the like.

The pseudomorphic forms of hydrated 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Forms II and IV) may be prepared by a variety of methodsas detailed below.

Ethyl Ester/Ketone to Form II

Hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form IV) may be prepared from ethyl 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-oxobutyl!-α,α-dimethylbenzeneacetate, hydrochloride orfree base as described above for the general preparation of thehydrated, pharmaceutically acceptable acid addition salts of thepiperidinoalkanol compounds of the formula (III) from the correspondingcompound of the formula (IV) wherein R₃ is --COOalkyl, and rapidlyadding water over a period of time ranging from 1 minute to 45 minutesat a temperature range of about -20° C. to 50° C. to precipitate thehydrated 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form II).

Ethyl Ester/Ketone to Form IV

Hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form IV) may be prepared from ethyl 4- 4-4-(hydroxydiphenylmethyl) -1-piperidinyl!-1-oxobutyl!-α,α-dimethylbenzeneacetate, hydrochloride or free base as described abovefor the general preparation of the hydrated, pharmaceutically acceptableacid addition salts of the piperidinoalkanol compounds of the formula(III) from the corresponding compound of the formula (IV) wherein R₃ is--COOalkyl, slowly adding water over a period of time ranging from about30 minutes to 24 hours and at a temperature range of about 0° C. to 50°C., optionally with seeding, to precipitate the hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form IV).

Form I to Form II

Hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form II) may be prepared from anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form I) by subjecting hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (Form II) to an aqueous recrystallization as definedabove.

Starting materials for use in the present invention are readilyavailable to one of ordinary skill in the art. For example, ethyl 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-oxobutyl!-α,α-dimethylbenzeneacetate,hydrochloride is described in U.S. Pat. No. 4,254,129, Mar. 3, 1981.

Preparation of the piperidinoalkanol compounds of formulas (I) through(IIIb) with the desired particle surface area is readily performed byone of ordinary skill in the art. For example, the particle surface areacan be increased by milling the piperidinoalkanol compounds with a JetMill (Jet-O-Mizer®, Fluid Energy Processing and Equipment Company,Hatfield, Pa.). Similar mills, such as the Micro-Jet (Fluid EnergyProcessing and Equipment Company) and the Sturtevant Micronize(Sturtevant, Boston, Mass.) may also be used. With the Jet Mill, thepiperidinoalkanol compound particles are accelerated in a millingchamber using compressed air. Piperidinoalkanol compound particlesurface area is increased by particle-to-particle impact. The mill isdesigned such that the particles exit the milling chamber and arecollected in a collection vessel. Fine particles are also collected in afilter bag. The particle surface area of the milled piperidinoalkanolcompound is influenced by the pressure of the compressed air and by thefeed of the piperidinoalkanol compound into the mill. Increased particlesurface area may also be achieved by controlled crystallization of thepiperidinoalkanol compound under conditions determined by one ofordinary skill in the art.

The particle surface area of the piperidinoalkanol compounds of formulas(I) through (IIIb) can be readily determined by one of ordinary skill inthe art. For example, the surface area can be determined by the BETmethod (see S. Brunauer, P. H. Emmet and E. Teller, J. Amer. Chem. Soc.,60(1938) 309-319). A gas adsorption instrument, such as the Quantasorb®Gas Sorption System (Quantachrome Corp., Syosset, N.Y. 11791) can beused to perform a multi-point analysis using nitrogen adsorption.

As used herein the term "inert ingredient" refers to thosetherapeutically inert ingredients that are well known in the art ofpharmaceutical science which can be used singly or in variouscombinations, and include, for example, binders, diluents, lubricants,glidants, sweetening agents, disintegrants, coloring agents, flavoringagents, antioxidants, solubilizing agents, coating agents and the like,as are disclosed in The United States Pharmacopeia, XXII, 1990, (1989The United States Pharmacopeial Convention, Inc.), pages 1857-1859,which is incorporated herein by reference. For example, the followinginert ingredients can be utilized singly or in various combinations;binders such as gelatin, polyvinylpyrrolidone (PVP), pregelatinizedstarch, povidone, cellulose derivatives including methyl cellulose,carboxymethyl cellulose, hydroxypropyl methylcellulose (HPMC),hydroxypropyl cellulose (HPC), sucrose and the like; diluents such ascalcium carbonate, lactose, starch, microcrystalline cellulose, and thelike; lubricants such as magnesium stearate, calcium stearate, zincstearate, stearic acid, talc, hydrogenated vegetable oil and the like;glidants such as silicon dioxide, talc and the like; disintegrants suchas alginic acid, methacrylic acid DVB, cross-linked PVP,microcrystalline cellulose, croscarmellose sodium, crospovidone,polacrilin potassium, sodium starch glycolate, starch, pregelatinizedstarch and the like; preferred disintegrants are croscarmellose sodium,starch, pregelatinized starch and sodium starch glycolate withcroscarmellose sodium being the most preferred disintegrant; sweeteningagents; coloring agents; flavoring agents; antioxidants; and the like.The above inert ingredients can be present in amounts up to about 95% ofthe total composition weight.

A suitable combination of inert ingredients comprises microcrystallinecellulose, pregelatinized starch, gelatin, magnesium stearate, calciumcarbonate and sodium starch glycolate, in amounts of from about 20% toabout 85%, 5% to about 50%, 1% to about 15%, 0.05% to about 3%, 5% toabout 50%, and 1% to about 15%. A preferred combination of inertingredients is microcrystalline cellulose, pregelatinized starch,calcium carbonate, magnesium stearate and sodium starch glycolate inamounts of from about 20% to about 85%, 5% to about 50%, 5% to about50%, 0.05% to about 3%, and 1% to about 15%. Another preferredcombination of inert ingredients comprises: microcrystalline cellulose,pregelatinized starch, magnesium stearate, and croscarmellose sodium inamounts of from about, 20% to about 85%, 5% to about 50%, 0.05 to about3%, 1% to about 10%. The most preferred combination of inert ingredientsis croscarmellose sodium, microcrystalline cellulose, lactose,pregelatinized starch and gelatin, in amounts of from about 1% to about10%, 20% to about 85%, 20% to about 85%, 1% to about 30% and 1% to about15% respectively. The most especially preferred combination of inertingredients is croscarmellose sodium, microcrystalline cellulose,lactose, pregelatinized starch, gelatin and magnesium stearate, inamounts of from about 1% to about 10%, 20% to about 85%, 20% to about85%, 1% to about 30%, 1% to about 15% and 0.05% to about 3%respectively. The following entries 1 through 7 in Table 5, provide themost preferred amounts of the respective inert ingredients which can beutilized in preparation of the tablet or capsule dosage forms;

                  TABLE 5                                                         ______________________________________                                        Preferred Amounts of Inert Ingredients                                        Preferred                                                                              #1     #2      #3    #4    #5   #6   #7                              Combination                                                                            (%)    (%)     (%)   (%)   (%)  (%)  (%)                             ______________________________________                                        Croscarmellose                                                                         4.8    4.8     --    --    4.8  6    --                              Sodium          (4.6)                                                         Microcrystal-                                                                          33.8   33.7    34.9  36.5  25.7 33.3 21.1                            line Cellulose  (32.4)  (33.5)                                                                              (35.1)                                          Lactose  33.8   33.7    --    --    25.7 --   --                                              (32.4)                                                        Pregelatinized                                                                         9.6    9.6     29.4  31.0  9.6  30   30                              Starch          (9.2)   (28.3)                                                                              (29.8)                                          Gelatin  3.5    3.5     3.3   --    3.5  --   --                                              (3.4)   (3.1)                                                 Magnesium                                                                              --     0.5     0.5   0.5   0.75 0.75 0.75                            Stearate        (0.5)   (0.5) (0.5)                                           Calcium  --     --      15.6  15.6  --   --   15.6                            Carbonate               (15.0)                                                                              (15.0)                                          Sodium Starch                                                                          --     --      5.6   5.6   --   --   10.0                            Glycolate               (5.4) (5.4)                                           ______________________________________                                    

The above entries in Table 5 represent percent by weight of thecomposition. The entries in parentheses for entries #2, #3, and #4represent the percent by weight of the composition after coating thetablet. It is understood by one of ordinary skill in the art that theabove combinations of inert ingredients, when combined with the chosenpiperidinoalkanol compound of formulas (I) through (IIIb), such as 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride or polymorphs, pseudomorphs or mixtures thereof, arethen manufactured in the chosen solid unit dosage form, such as acapsule or tablet, utilizing techniques well known in the art ofpharmaceutical science.

In general, solid unit dosage forms of the present invention can beformulated and manufactured in capsule form using the followingprocedure:

The desired inert ingredients are blended together with thepiperidinoalkanol compound of formulas (I) through (IIIb) utilizingtechniques and procedures well known to one of ordinary skill in theart. For example, microcrystalline cellulose, lactose, pregelatinizedstarch and a piperidinoalkanol compound of formulas (I) through (IIIb),such as 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of greater than about 1m² /g, are blended together. A solution of gelatin in water is added andmixed in with the powder blend. The resulting wet granulation is thendried and milled to uniform size. Croscarmellose sodium is then added tothe milled granulation and blended to produce the final granulation.This granulation is then filled into hard gelatin capsules underconventional conditions as is well known to one of ordinary skill in theart.

In general, solid unit dosage forms of the present invention can beformulated and manufactured in tablet form using one of the followingprocedures:

The desired inert ingredients are blended together with thepiperidinoalkanol compound of formulas (I) through (IIIb) utilizingtechniques and procedures well known to one of ordinary skill in theart. For example, microcrystalline cellulose, lactose, pregelatinizedstarch and a piperidinoalkanol compound of formulas (I) through (IIIb),such as 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride or polymorphs, pseudomorphs or mixtures thereof, witha particle surface area of greater than about 1.0 m² /g, are blendedtogether. A solution of gelatin in water is added and mixed in with thepowder blend. The resulting wet granulation is then dried and milled touniform size. Croscarmellose sodium and magnesium stearate are thenadded to the milled granulation and blended to produce the finalgranulation. This granulation is then compressed into tablets underconventional conditions as is well known to one of ordinary skill in theart. The compressed tablets can be film coated using standardingredients and procedures commonly used and well known in the art ofpharmaceutical science.

In an additional general procedure, microcrystalline cellulose, thepregelatinized starch, part of the croscarmellose sodium and apiperidinoalkanol compounds of formulas (I) through (IIIb), such as 4-4- 4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride are blended together. Water is added and mixed with thepowder blend. The resulting wet granulation is then dried and milled toa uniform size. Additional microcrystalline cellulose and croscarmellosesodium are added to the granulation and blended. Finally, magnesiumstearate is added and blended with the mixture to produce the finalgranulation. This granulation is then compressed into tablets underconventional conditions well known to one of ordinary skill in the art.The compressed tablets can be film coated using standard ingredients andprocedures used and well known in the art of pharmaceutical science.

Another example would include blending microcrystalline cellulose, thepregelatinized starch, the calcium carbonate, part of the sodium starchglycolate, and a compound of formulas (I) through (IIIb), such as 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride or polymorphs, pseudomorphs or mixtures thereof. Water isadded and mixed with the powder blend. The resulting wet granulation isthen dried and milled to a uniform size. Additional microcrystallinecellulose and the remaining sodium starch glycolate are blendedtogether. The resulting mixture is blended with the magnesium stearateto produce the final granulation. This granulation is then compressedinto tablets under conventional conditions well known to one of ordinaryskill in the art. The compressed tablets can be filmed coated usingstandard ingredients and procedures used and well known in the art ofpharmaceutical science.

The above procedures may also be used for preparation of solid unitdosage forms wherein the piperidinoalkanol compound of formulas (I)through (IIIb), such as 4- 4- 4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride or polymorphs, pseudomorphs or mixtures thereof, has aparticle surface area less than about 1 m² /g.

For the entries 1 through 4 in Table 5, wherein the solid unit dosageform is a tablet, the quantity of compound of the formula; ##STR8##wherein X is a number ranging from about zero to 5, and the individualoptical isomers thereof, dissolved in 45 minutes, is not less than 75%of label in water, at a temperature of about 37° C. and about 50 rpmwhen measured according to USP Apparatus 2 as is disclosed in the UnitedStates Pharmacopeia, 23, U.S. Pharmacopeial Convention, Inc., Rockville,Md., 20852 (1995), pages 1791-1793 which is hereby incorporated byreference.

For the entries 5 through 7 in Table 5, wherein the solid unit dosageform is a tablet, the quantity of compound of the formula; ##STR9##wherein X is a number ranging from about zero to 5, and the individualoptical isomers thereof, dissolved in 45 minutes, is not less than 75%of label in 0.001N aqueous hydrochloric acid, at a temperature of about37° C. and about 50 rpm when measured according to USP Apparatus 2 as isdisclosed in the United States Pharmacopeia, 23, U.S. PharmacopeialConvention, Inc., Rockville, Md., 20852 (1995), pages 1791-1793, whichis hereby incorporated by reference.

The following examples are understood to be illustrative only and arenot intended to limit the scope of the present invention in any way. Thereagents and starting materials are available to one of ordinary skillin the art. As used herein, the following terms have the indicatedmeanings: "m² /g" refers to square meters per gram and is used as ameasurement of particle surface area; "kg" refers to kilograms; "g"refers to grams; "mmol" refers to millimoles; "ml" refers tomilliliters; "bp" refers to boiling point; "mp" refers to melting point;"°C." refers to degrees Celsius; "°F." refers to degrees Fahrenheit; "mmHg" refers to millimeters of mercury; "μL" refers to micro-liters; and"μg" refers to micrograms.

EXAMPLE 1 20 mg Gelatin Capsules for Oral Administration

Combine 32.4 kg of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m² /g, 76.1kg microcrystalline cellulose, 76.1 kg lactose, and 21.6 kgpregelatinized starch and blend in a mixer for 5 minutes. To thismixture, add a solution of 7.9 kg of gelatin in 55.0 kg purified water(prepared by adding the gelatin to the water and heating the dispersionwith mixing until solution of the gelatin is attained) and continuemixing until a good granulation is formed. Pass the granulation througha 0.375 inch screen and dry at 60° C. until a moisture content of lessthan 3.0% is achieved as determined by a Computrac moisture balance at125° C. Mill the dried granulation through a 0.065 inch screen. To thegranulation add 10.8 kg of croscarmellose sodium and mix for about 10minutes. Fill the granulation into size 3 hard gelatin capsules to afill weight of 138.9 mg granulation per capsule. This procedure resultsin about 1,620,000 capsules of the composition shown in table 6 below.

                  TABLE 6                                                         ______________________________________                                        Composition of 20 mg Gelatin Capsules.                                                         AMOUNT    COMPOSITION                                        INGREDIENT       mg/capsule                                                                              % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    20.0      14.4                                               Microcrystalline Cellulose                                                                     47.0      33.8                                               Lactose          47.0      33.8                                               Pregelatinized Starch                                                                          13.3      9.6                                                Croscarmellose Sodium                                                                          6.7       4.8                                                Gelatin          4.9       3.5                                                ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 2 30 mg Capsules for Oral Administration

Combine 144.0 g of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m² /g,338.5 g microcrystalline cellulose, 338.5 g lactose, and 96.0 gpregelatinized starch in a blender and blend. To the powder blend, add asolution of 35.0 g of gelatin in 286.1 g of purified water (prepared byadding the gelatin to the water and heating the dispersion with mixinguntil solution of the gelatin is attained) and continue mixing until agood granulation is formed. Pass the granulation through a screen, ifnecessary, and dry the granulation. Mill the dried granulation. To themilled granulation in a blender, add 48.0 g of croscarmellose sodium andblend. Fill the finished granulation into size 1 hard gelatin capsulesto the desired weight. This procedure results in 4801 capsules each witha total fill weight of 208.3 mg with the composition shown in table 7below.

                  TABLE 7                                                         ______________________________________                                        Composition of 30 mg Capsules.                                                                 AMOUNT    COMPOSITION                                        INGREDIENT       mg/capsule                                                                              % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    30.0      14.4                                               Microcrystalline Cellulose                                                                     70.5      33.8                                               Lactose          70.5      33.8                                               Pregelatinized Starch                                                                          20.0      9.6                                                Gelatin          7.3       3.5                                                Croscarmellose Sodium                                                                          10.0      4.8                                                ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 3 30 mg Capsules for Oral Administration

Combine 144.1 g of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m² /g,338.5 g microcrystalline cellulose, 338.5 g lactose, and 96.0 gpregelatinized starch in a blender and blend. To the powder blend, add asolution of 35.1 g of gelatin in 286.2 g of purified water (prepared byadding the gelatin to the water and heating the dispersion with mixinguntil solution of the gelatin is attained) and continue mixing until agood granulation is formed. Pass the granulation through a screen, ifnecessary, and dry the granulation. Mill the dried granulation. To themilled granulation in a blender, add 48.0 g of croscarmellose sodium andblend. Add 4.8 g of magnesium stearate to the blend and blend further.Fill the finished granulation into size 1 hard gelatin capsules to thedesired weight. This procedure results in 4802 capsules each with atotal fill weight of 209.3 mg with the composition shown in table 8below.

                  TABLE 8                                                         ______________________________________                                        Composition of 30 mg Capsules.                                                                 AMOUNT    COMPOSITION                                        INGREDIENT       mg/capsule                                                                              % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    30.0      14.3                                               Microcrystalline Cellulose                                                                     70.5      33.7                                               Lactose          70.5      33.7                                               Pregelatinized Starch                                                                          20.0      9.6                                                Gelatin          7.3       3.5                                                Croscarmellose Sodium                                                                          10.0      4.8                                                Magnesium Stearate                                                                             1.0       0.5                                                ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 4 40 mg Gelatin Capsules for Oral Administration

Combine 32.4 kg of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m² /g, 76.1kg microcrystalline cellulose, 76.1 kg lactose, and 21.6 kgpregelatinized starch and blend in a mixer for 5 minutes. To thismixture, add a solution of 7.9 kg of gelatin in 55.0 kg purified water(prepared by adding the gelatin to the water and heating the dispersionwith mixing until solution of the gelatin is attained) and continuemixing until a good granulation is formed. Pass the granulation througha 0.375 inch screen and dry at 60° C. until a moisture content of lessthan 3.0% is achieved as determined by a Computrac moisture balance at125° C. Mill the dried granulation through a 0.065 inch screen. To thegranulation add 10.8 kg of croscarmellose sodium and mix for about 10minutes. Fill the granulation into size 1 hard gelatin capsules to atotal fill weight of 277.8 mg granulation per capsule. This procedureresults in about 810,000 capsules of the composition shown in table 9below.

                  TABLE 9                                                         ______________________________________                                        Composition of 40 mg Gelatin Capsules.                                                         AMOUNT    COMPOSITION                                        INGREDIENT       mg/capsule                                                                              % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    40.0      14.4                                               Microcrystalline Cellulose                                                                     94.0      33.8                                               Lactose          94.0      33.8                                               Pregelatinized Starch                                                                          26.6      9.6                                                Croscarmellose Sodium                                                                          13.3      4.8                                                Gelatin          9.8       3.5                                                ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 5 60 mg Gelatin Capsules For Oral Administration

Combine 32.4 kg of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m² /g, 76.1kg microcrystalline cellulose, 76.1 kg lactose, and 21.6 kgpregelatinized starch and blend in a mixer for 5 minutes. To thismixture, add a solution of 7.9 kg of gelatin in 55.0 kg purified water(prepared by adding the gelatin to the water and heating the dispersionwith mixing until solution of the gelatin is attained) and continuemixing until a good granulation is formed. Pass the granulation througha 0,375 inch screen and dry at 60° C. until a moisture content of lessthan 3.0% is achieved as determined by a Computrac moisture balance at125° C. Mill the dried granulation through a 0.065 inch screen. To thegranulation add 10.8 kg of croscarmellose sodium and mix for about 10minutes. Fill the granulation into size 0 hard gelatin capsules to atotal fill weight of 416.7 mg granulation per capsule. This procedureresults in about 540,000 capsules off the composition shown in table 10below.

                  TABLE 10                                                        ______________________________________                                        Composition of 60 mg Capsules.                                                                 AMOUNT    COMPOSITION                                        INGREDIENT       mg/capsule                                                                              % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    60.0      14.4                                               Microcrystalline Cellulose                                                                     141.0     33.8                                               Lactose          141.0     33.8                                               Pregelatinized Starch                                                                          40.0      9.6                                                Croscarmellose Sodium                                                                          20.0      4.8                                                Gelatin          14.7      3.5                                                ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 6 30 mg Tablets For Oral Administration

Combine 144.1 g of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m² /g,338.5 g microcrystalline cellulose, 338.5 g lactose, and 96.0 gpregelatinized starch and blend in a mixer for 5 minutes. To the powderblend, add a solution of 35.1 g of gelatin in 286.2 g purified water(prepared by adding the gelatin to the water and heating the dispersionwith mixing until solution of the gelatin is attained) and continuemixing until a good granulation is formed. Pass the granulation througha screen, if necessary and dry the granulation. Mill the driedgranulation, add 48.0 g of croscarmellose sodium and mix in a blender.Then add 4.8 g of magnesium stearate to the blender and blend further.Compress the finished granulation into tablets. Place the tablets into acoating pan and coat the tablets with a dispersion of 30.3 g of OpadryYS-1-18027-A (Colorcon, West Point Pa.) in 138.0 g of water and adispersion of 10.6 g of Opadry YS-1-19016 (Colorcon, West Point Pa.) in121.9 g of water. This procedure results in 4802 tablets each with atotal weight of 217.8 mg with the composition shown in table 11 below.The percentages in parentheses in table 11 represent the percent byweight of the composition after coating the tablet.

                  TABLE 11                                                        ______________________________________                                        Composition of 30 mg Tablets.                                                                  AMOUNT    COMPOSITION                                        INGREDIENT       mg/tablet % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    30.0      14.3 (13.8)                                        Microcrystalline Cellulose                                                                     70.5      33.7 (32.4)                                        Lactose          70.5      33.7 (32.4)                                        Pregelatinized Starch                                                                          20.0      9.6 (9.2)                                          Croscarmellose Sodium                                                                          10.0      4.8 (4.6)                                          Gelatin          7.3       3.5 (3.4)                                          Magnesium Stearate                                                                             1.0       0.5 (0.5)                                          Opadry YS-1-18027-A                                                                            6.3        -- (2.9)                                          Opadry YS-1-19016                                                                              2.2        -- (1.0)                                          ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 7 30 mg Tablets for Oral Administration

Combine 149.9 g of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m² /g,214.2 g microcrystalline cellulose, 218.7 g calcium carbonate, and 411.6g pregelatinized starch in a blender and blend. To the powder blend, adda solution of 45.5 g of gelatin in 400.0 g of purified water (preparedby adding the gelatin to the water and heating the dispersion withmixing until solution of the gelatin is attained) and continue mixinguntil a good granulation is formed. Pass the granulation through ascreen, if necessary, and dry the granulation. Screen the remainingmicrocrystalline cellulose and add the 274.1 g of microcrystallinecellulose with 78.3 g sodium starch glycolate to the dried granulationin a blender and blend. Screen the magnesium stearate and add the 7.5 gof magnesium stearate to the blend and blend further. Compress thefinished granulation into tablets. Place the tablets into a coating panand coat the tablets with a dispersion of 42.0 g of Opadry YS-1-18027-A(Colorcon, West Point Pa.) in 191.0 g of water and a dispersion of 14.5g of Opadry YS-1-19016 (Colorcon, West Point Pa.) in 166.8 g of water.This procedure results in 4999 tablets each with a total weight of 291.3mg with the composition shown in table 12 below. The percentages inparentheses in table 12 represent the percent by weight of thecomposition after coating the tablet.

                  TABLE 12                                                        ______________________________________                                        Composition of 30 mg Tablets.                                                                  AMOUNT    COMPOSITION                                        INGREDIENT       mg/tablet % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    30.0      10.7 (10.3)                                        Microcrystalline Cellulose                                                                     97.7      34.9 (33.5)                                        Calcium Carbonate                                                                              43.7      15.6 (15.0)                                        Pregelatinized Starch                                                                          82.3      29.4 (28.3)                                        Gelatin          9.1       3.3 (3.1)                                          Sodium Starch Glycolate                                                                        15.7      5.6 (5.4)                                          Magnesium Stearate                                                                             1.5       0.5 (0.5)                                          Opadry YS-1-18027-A                                                                            8.4        -- (2.9)                                          Opadry YS-1-19016                                                                              2.9        -- (1.0)                                          ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 8 30 mg Tablets for Oral Administration

Combine 149.9 g of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2-4 m2/g, 214.2g microcrystalline cellulose, 218.7 g calcium carbonate, and 434.3 gpregelatinized starch in a blender and blend. To the powder blend, add460.0 g of purified water and blend until a good granulation is formed.Pass the granulation through a screen, if necessary, and dry thegranulation. Screen the remaining microcrystalline cellulose and add the296.8 g of microcrystalline cellulose with 78.3 g sodium starchglycolate to the dried granulation in a blender and blend. Screen themagnesium stearate and add the 7.5 g of magnesium stearate to the blendand blend further. Compress the finished granulation into tablets. Placethe tablets into a coating pan and coat the tablets with a dispersion of42.0 g of Opadry YS-1-18027-A (Colorcon, West Point Pa.) in 191.3 g ofwater and a dispersion of 14.5 g of Opadry YS-1-19016 (Colorcon, WestPoint Pa.) in 166.8 g water. This procedure results in 4999 tablets eachwith a total weight of 291.3 mg with the composition shown in table 13below. The percentages in parentheses in table 13 represent the percentby weight of the composition after coating the tablet.

                  TABLE 13                                                        ______________________________________                                        Composition of 30 mg Tablets.                                                                  AMOUNT    COMPOSITION                                        INGREDIENT       mg/tablet % by weight                                        ______________________________________                                        Piperidinoalkanol Compound*                                                                    30.0      10.7 (10.3)                                        Microcrystalline Cellulose                                                                     102.2     36.5 (35.1)                                        Calcium Carbonate                                                                              43.7      15.6 (15.0)                                        Pregelatinized Starch                                                                          86.9      31.0 (29.8)                                        Sodium Starch Glycolate                                                                        15.7      5.6 (5.4)                                          Magnesium Stearate                                                                             1.5       0.5 (0.5)                                          Opadry YS-1-18027-A                                                                            8.4        -- (2.9)                                          Opadry YS-1-19016                                                                              2.9        -- (1.0)                                          ______________________________________                                         *4- 4 4(Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 9

In a manner analogous to the procedures described in examples 1 through8, the respective tablets and capsules can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2 m² /g toabout 6 m² /g.

EXAMPLE 10

In a manner analogous to the procedures described in examples 1 through8, the respective tablets and capsules can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2 m2/g to about10 m² /g.

EXAMPLE 11

In a manner analogous to the procedures described in examples 1 through8, the respective tablets and capsules can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area greater than about 1m2/g.

EXAMPLE 12

In a manner analogous to the procedures described in examples 1 through8, the respective tablets and capsules can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride which has not been subjected to micronization suchthat the 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride has a particle surface area of less than about 1.0 m² /g.

EXAMPLE 13

Utilizing the procedures described in examples 1 through 12, the tabletsand capsules may contain 4- 4- 4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride in amounts from about 5 mg to about 120 mg. The 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride and inert ingredients are present in the describedpercentage amounts by weight, which are readily determined by one ofordinary skill in the art from the previous examples. For example, oneof ordinary skill in the art, following the procedures of examples 1through 12 in an analogous manner, can prepare tablets and capsules, inaddition to those already set forth, wherein 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride is present in amounts of 10 mg, 20 mg, 30 mg, 40 mg,50 mg, 60 mg, 70 mg, 80 mg, 90 mg, 100 mg, 110 mg and 120 mg.

EXAMPLE 14 180 mg Tablet for Oral Administration

Combine 180.0 g of 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride, 78.0 g of microcrystalline cellulose (Avicel PH101)180.0 g of pregelatinized starch, and part of the 36.0 g of the sodiumcroscarmellose in a blender and blend. To the powder blend, add 180 g ofpurified water and mix. Dry the resulting wet granulation. Screen thedried granulation through a 20 mesh screen. Transfer the granulation toa blender and add 121.5 g of microcrystalline cellulose (Avicel PH102)and the remaining amount of the Sodium Croscarmellose. Blend thesecomponents. Add 4.5 g of magnesium stearate and blend. Compress thefinished granulation into tablets. Table 14 provides the composition ofeach tablet in percent by weight prior to coating the tablet.

To coat the compressed tablets with a peach aqueous coating, prepare anaqueous suspension comprised of 2.84 g of hydroxypropyl methyl cellulose(USP2910 E-15), 1.89 g of hydroxypropyl methyl cellulose (USP2910 E-5)0.51. g of Povidone (USP), 2.02 g of titanium dioxide (USP), 0.025 g ofpink iron oxide blend, 0.04 g of yellow iron oxide blend, 0.73 g ofsilicone dioxide (M7) 3.94 g of polyethylene glycol 400 (N.F.), andabout 88 g of purified water. Place the tablets into a coating pan andcoat the tablets using the peach aqueous suspension to achieve about a3% weight gain. This procedure provides a tablet with a total weight of618.0 mg.

                  TABLE 14                                                        ______________________________________                                        Composition of 180 mg Tablets.                                                                 Amount    Composition                                        INGREDIENT       mg/tablet % Weight                                           ______________________________________                                        Piperidinoalkanol Compound*                                                                    180.0     30.0                                               Microcrystalline Cellulose                                                                     199.5     33.3                                               Pregelatinized Starch                                                                          180.0     30.0                                               Croscarmellose Sodium                                                                          36.0      6.0                                                Magnesium Stearate                                                                             4.5       0.75                                               ______________________________________                                         *4- 4 4(hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutyl-α,dimeth    lbenzeneacetic acid hydrochloride with a particle surface area of about 2-     m.sup.2 /g.                                                              

EXAMPLE 15 180 mg Tablet for Oral Administration

Combine 180.0 g of 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride, 84.5 g of microcrystalline cellulose (Avicel PH101),240 g of pregelatinized starch, 125.0 g of calcium carbonate (Heavy),and part of the 80.0 g of the Sodium starch glycolate in a blender andblend. To the powder mix, add 224 g of water and mix. Dry the resultingwet granulation. Screen the dried granulation through a 20 mesh screen.Transfer the granulation to a blender. Add 84.5 g of microcrystallinecellulose (Avicel PH102) and the remaining amount of the sodium starchglycolate. Blend these components. Add 6.0 g of magnesium stearate andblend. Compress the finished granulation into Tablets. Table 15 providesthe composition of each tablet in percent by weight prior to coating thetablet.

To coat the compressed tablets with a white aqueous coating, prepare anaqueous suspension comprised of 2.84 g of hydroxypropyl methyl cellulose(USP2910 E-15), 1.89 g of hydroxypropyl methyl cellulose (USP2910E-5)0.51 g of Povidone (USP), 2.1 g of titanium dioxide (USP), 0.73 g ofsilicone dioxide (M7) 3.94 g of polyethylene glycol 400 (N.F.), andabout 88 g of purified water. Place the tablets into a coating pan andcoat the tablets using the white aqueous suspension to achieve about a3% weight gain. This procedure provides a tablet with a total weight of

                  TABLE 15                                                        ______________________________________                                        Composition of 180 mg Tablets.                                                                   Amount   Composition                                       INGREDIENT         mg/tablet                                                                              % weight                                          ______________________________________                                        Piperidinoalkanol Compound*                                                                      180.0  mg    22.5                                          Microcrystalline Cellulose                                                                       169.0        21.1                                          Pregelatinized Starch                                                                            240.0        30.0                                          Sodium Starch glycolate                                                                          80.0         10.0                                          Calcium Carbonate  125.0        15.6                                          Magnesium Stearate Special                                                                       6.0          0.75                                          ______________________________________                                         *4- 4 4(hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutyl)-α,dimet    ylbenzeneacetic acid hydrochloride with a particle surface area of about       2-4 m.sup.2 /g.                                                          

EXAMPLE 16 180 mg Tablet for Oral Administration

Combine 180.0 g of 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride, 154.0 g of microcrystalline cellulose (AvicelPH101), 57.5 g of pregelatinized starch, and 154 g of lactose (hydrous,Fast-Flo) in a blender and blend. Prepare a granulating liquid by adding21.2 g of gelatin to 142 g of water and heating the dispersion.

Add the granulating liquid to the powder blend and mix. Dry theresulting wet granulation. Screen the dried granulation through a 20mesh screen. Transfer the granulation to a blender. Add 28.8 g of SodiumCroscarmellose to the granulation and blend. Add 4.5 g of magnesiumstearate to the granulation and blend. Compress the finished granulationinto tablets. Table 16 provides the composition of each tablet inpercent by weight prior to coating the tablet.

The finished tablets may be coated in a manner analogous to thosedescribed in example 14 with the peach aqueous coating or in example 15with the white aqueous coating.

                  TABLE 16                                                        ______________________________________                                        Composition of 180 mg Tablets.                                                                  Amount   Composition                                        INGREDIENT        mg/tablet                                                                              % Weight                                           ______________________________________                                        Piperidinoalkanol Compound*                                                                     180.0    30.0                                               Microcrystalline Cellulose                                                                      154      25.7                                               pregelatinzed starch                                                                            57.5     9.6                                                Lactose           154.0    25.7                                               Gelatin           21.2     3.5                                                Sodium Croscarmellose                                                                           28.8     4.8                                                Magnesium Stearate                                                                              4.5      0.75                                               ______________________________________                                         *4- 4 4(hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethy    benzeneacetic acid hydrochloride with a particle surface area of about 2-4     m.sup.2 /g.                                                              

EXAMPLE 17 60 mg Tablets for Oral Administration

Combine 60 g of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride 141.0 g of microcrystalline cellulose, 141.0 glactose, and 40 g pregelatinized starch and blend in a mixer. To thismixture, add a solution of 14.7 g of gelatin in 101.9 g purified water(prepared by adding the gelatin to the water and heating the dispersionwith mixing until solution of the gelatin is attained) and continuemixing until a granulation is formed. Pass the granulation through ascreen and dry. To the granulation add 20.0 g of croscarmellose sodiumand mix. Then add 2.1 g of magnesium stearate to the blend and blendfurther. Compress the finished granulation into tablets. Table 17provides the composition of each tablet in percent by weight prior tocoating the tablet.

The resulting tablets may be coated in a manner analogous to thatdescribed in example 6 with Opadry YS-1-18027-A and Opadry YS-1-19016.Alternatively, the resulting tablets may be coated in a manner analogousto that described in example 14 with the peach aqueous coating or inexample 15 with the white aqueous coating.

                  TABLE 17                                                        ______________________________________                                        Composition of 60 mg Tablets.                                                                    Amount   Composition                                       INGREDIENT         mg/tablet                                                                              % Weight                                          ______________________________________                                        Piperidinoalkanol Compund*                                                                       60.0     14.3                                              Microcrystalline Cellulose                                                                       141.0    33.7                                              Lactose            141.0    33.7                                              Pregelatinized Starch                                                                            40.0     9.6                                               Sodium Croscarmellose                                                                            20.0     4.8                                               Gelatin            14.7     3.5                                               Magnesium Stearate 2.1      0.5                                               ______________________________________                                         *4- 4 4Hydroxydiphenylmethyl)-1-piperidinyl1-hydroxybutylα,dimethyl    enzeneacetic acid hydrochloride with a particle surface area of about 2-4      m.sup.2 /g.                                                              

EXAMPLE 18

In a manner analogous to the procedures described in examples 14 through17, the tablets can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2 m² /g toabout 6 m² /g.

EXAMPLE 19

In a manner analogous to the procedures described in examples 14 through17, the tablets can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area of about 2 m² /g toabout 10 m² /g.

EXAMPLE 20

In a manner analogous to the procedures described in examples 14 through17, the tablets can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride with a particle surface area greater than about 1 m²/g.

EXAMPLE 21

In a manner analogous to the procedures described in examples 14 through17, the respective tablets and capsules can be prepared utilizing 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride which has not been subjected to micronization suchthat the 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride has a particle surface area of less than about 1.0 m² /g.

The following examples present typical processes for preparing theanhydrous and hydrated, pharmaceutically acceptable acid addition saltsof the piperidinoalkanol compounds of the formulas (III) and (IIIa),polymorphs and pseudomorphs thereof. These examples are understood to beillustrative only and are not intended to limit the scope of the presentinvention in any way.

Differential Scanning Calorimetry analysis were performed using a TA2910 DSC with open aluminum pans. The samples were heated to 240° C. at5° C./minute with a 50 mL/minute nitrogen purge.

X-Ray Powder Diffraction analyses were performed as follows:

The samples were loaded into a quartz (zero scatter) sample holder forthe XRPD pattern measurement. The XRPD patterns were measured using apowder diffractometer equipped with a Co X-ray tube source, primary beammonochromator, and position sensitive detector (PSD). The incident beamwas collimated using a 1° divergence slit. The active area on the PSDsubtended approximately 5° 2⊖. The source was operated at 35 kV and 30mA and the sample was illuminated with Co Kα₁ radiation. XRPD data werecollected from 5° to 55° 2⊖ at a rate of 0.25° 2⊖/minute and a stepwidth of 0.02° 2⊖. The XRPD patterns were measured without the additionof an internal calibrant.

Peak positions and intensities for the most prominent features weremeasured using a double-derivative peak picking method. X-ray peaks withI/I_(o) greater than 20% were reported. The cutoff was chosenarbitrarily. The intensities are rounded to the nearest 5%. Certainpeaks appear sensitive to preferred orientation that is caused bychanges in crystallite morphology. This results in large changes in theI/I_(o) value.

EXAMPLE 22 Preparation of Form II 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride

Method A

Mix ethyl 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-oxobutyl!-α,α-dimethylbenzeneacetate,hydrochloride (101.92 g, 0.1807 mol) and methanol (510 mL) and stir.Rapidly add 50% sodium hydroxide (72.27 g, 0.903 mol) and wash in withwater (61 mL). Heat to reflux for 2 hours, allow to cool to 35° C. andtreat with sodium borohydride (3.42 g, 0.0903 mol). Add water (100 mL)and maintain at 35° C. for 10 hours. Add 37% hydrochloric acid (53.0 g)to adjust pH to 11.5. Add acetone (26.5 mL) and water (102 mL). Hold at35° C. for 2 hours and adjust to pH 2.5 with 37% hydrochloric acid(44.69 g). Dilute with water (408 mL), cool to -15° C., stir for 1.5hours and collect the precipitate by vacuum filtration. Wash thefiltercake with deionized water (3×100 mL) and vacuum dry to give 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride hydrate (97.10 g).

Method B

Place ethyl 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-oxobutyl!-α,α-dimethylbenzeneacetate,hydrochloride (60.01 g, 0.106 mol) in a 1-L three necked round-bottomflask and fit the flask with a mechanical stirrer, a Claisen head, athermometer and a reflux condenser with a nitrogen bubbler on top. Addmethanol (300 mL) and turn the stirrer on. Dilute the slurry with water(60 mL) and heat to 52-54° C. over 15-20 minutes. Hold at 52° C. for 2hours and then add 50% sodium hydroxide (42.54 g, 0.532 mol). Heat at73° C. for approximately 1 hour, 45 minutes, cool to less than 35° C.using a water bath and then add sodium borohydride (2.02 g, 0.0534 mol).Stir overnight at 35° C., treat with acetone (15.5 mL) and stir for 2hours at 35° C. Acidify the mixture to a pH of 1.85 with 28%hydrochloric acid (75.72 g), dilute with water (282 mL), stir for about30 minutes and cool over about 2 hours to -15° C. Filter the solids offand wash with water (2×75 mL) and ethyl acetate (2×75 mL). Vacuum drythe solid and allow to stand for 2 days to give 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride hydrate (Form II) (57.97 g, 91.5%) as a fine powder.

Method C

Place ethyl 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-oxobutyl!-α,α-dimethylbenzeneacetate(56.12 g, 0.1064 mol) in a 1-L three necked round-bottom flask and fitthe flask with a mechanical stirrer, a Claisen head, a thermometer and areflux condenser with a nitrogen bubbler on top. Add methanol (300 mL)and turn the stirrer on. Dilute the slurry with water (60 mL) and heatto reflux using a heating mantle controlled by a Therm-O-Watch. When themixture reaches about 35° C., treat with 50% sodium hydroxide (34.05 g,0.4256 mol) and rinse in with water (42 mL). Stir at reflux for 2 hours,15 minutes, cool over 1 hour to 35° C. and then treat with sodiumborohydride (2.02 g, 0.0534 mol). Stir for 7.5 hours and allow to standat room temperature without stirring for 1.75 days. Warm the mixture to35° C. and quench with acetone (15.5 mL, 0.21 mol) and stir for 2 hours.Add water (60 mL) and adjust the pH to 2.5 with 32% hydrochloric acid(65.22 g). Cool to 40° C. and rinse the pH probe with water (25 mL). Addwater over about 30 minutes (192 mL), hold the temperature at 33° C. for10 minutes and add a few seed crystals. Cool the slurry to -12° C. overabout 45 minutes and isolate the solid by filtration (586.2 g). Washwith water (2×100 mL) and then with ethyl acetate (100 ml, prechilled toabout -10° C.). Vacuum dry overnight (1 mmHg, 50° C.) to give 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form II) (58.86 g 98%) as a white solid.

EXAMPLE 23 Preparation of Form IV 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!1!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride

(Form IV)

Place ethyl 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-oxobutyl!-α,α-dimethylbenzeneacetate(56.12 g, 0.1064 mol) in a 1-L three necked round-bottom flask and fitthe flask with a mechanical stirrer, a Claisen head, a thermometer and areflux condenser with a nitrogen bubbler on top. Add methanol (300 mL)and turn the stirrer on. Dilute the slurry with water (60 mL) and heatto reflux using a heating mantle controlled by a Therm-O-Watch. When themixture reaches about 35° C., treat with 50% sodium hydroxide (34.05 g,0.4256 mol) and rinse in with water (42 mL). Stir at reflux for 2 hours,15 minutes, cool over 1 hour to 35° C. and then treat with sodiumborohydride (2.02 g, 0.0534 mol). Stir for 7.5 hours and allow to standat room temperature without stirring for 1.75 days. Warm the mixture to35° C. and quench with acetone (15.mL, 0.21 mol) and stir for 2 hours.Add water (60 mL) and adjust the pH to 2.5 with 32% hydrochloric acid(65.22 g). Cool to 40° C. and rinse the pH probe with water (25 mL).Hold the temperature at 33° C. for 10 minutes, add a few seed crystalsand add water over about 4 hours (192 mL) at 35° C. Cool the slurry to-12° C. over about 45 minutes and isolate the solid by filtration (586.2g). Wash with water (2×100 mL) and then with ethyl acetate (100 mL,prechilled to about -10° C.). Vacuum dry overnight (1 mmHg, 50° C.) togive 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-.alpha.,α-dimethylbenzeneaceticacid hydrochloride hydrate (Form IV); mp 115°-116° C. (dec). XRPD: Table18

                  TABLE 18                                                        ______________________________________                                        D-Space,                                                                      Angstroms    Intensity, I/I.sub.O, %                                          ______________________________________                                        10.38        60                                                               6.97         45                                                               6.41         50                                                               5.55         30                                                               5.32         100                                                              5.23         55                                                               5.11         35                                                               4.98         25                                                               4.64         30                                                               4.32         35                                                               4.28         75                                                               4.12         50                                                               4.02         45                                                               3.83         60                                                               3.65         20                                                               3.51         55                                                               3.46         25                                                               2.83         20                                                               ______________________________________                                    

EXAMPLE 24 Conversion of Form II to Form I 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride

(Form I)

Treat 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form II) (20.0 g, 0.0355 mol) with deionizedwater (2 g) and add acetone (60 mL) in small portions over severalminutes with stirring. Filter through filter aid and wash the filtercake with acetone (30 mL). Wash the filtercake with acetone (22 mL),reflux filtrate and then slowly add ethyl acetate (32 mL over 15minutes) keeping the mixture at reflux. Reflux for 10 minutes, thenslowly add additional ethyl acetate (23 mL over 10 minutes) and refluxfor an additional 15 minutes. Add additional ethyl acetate (60 mL over5-10 minutes) and continue refluxing for 15 minutes. Cool toapproximately 8° C. in an ice bath, filter the solid and wash with ethylacetate (85 mL). Vacuum dry at 55° C. for 1.5 hours to give the titlecompound (18.16 g, 95%).

EXAMPLE 25 Conversion of Form II to Form I 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride

Method A

Treat 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form II) (5.00 g, 0.0083 mol) withmethylethyl ketone (130 mL). Slowly add water (0.4 mL), filter throughfilter aid and wash the filter cake with methylethyl ketone (20 mL).Heat to reflux and distill off 75 mL of solvent, cool to -15° C. andcollect by vacuum filtration. Wash with methylethyl ketone (2×10 mL) andvacuum dry at 60° C. to give the title compound (4.33 g, 97%); mp196°-198° C.

Method B

Treat 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form II) (1.4 g) with acetone (60 mL) andheat to reflux. Reduce the volume to approximately 35 mL to remove allwater which boils off as an azeotrope (88/12: acetone/water). Cool thesolution and collect the title compound as a crystalline solid.

Method C

Mix 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form II) (53.88 g, 0.100 mol) and add water(4.79 g) and methyl ethyl ketone (240 mL). Stir until the solid isslurried up and add additional methyl ethyl ketone (1 L). Stir for 0.5hours, filter through a pad of filter aid, wash the filtercake withmethyl ethyl ketone (100 mL) and transfer the filtrate and wash to a 2L, 3-necked flask fitted with a thermometer, mechanical stirrer anddistillation head. Distill off a total of 721 mL of methyl ethyl ketone,cool and stir over 1 hour to 40° C. Cool to -15° C. and hold for 10minutes. Collect the solid by vacuum filtration and wash the filtercakewith methyl ethyl ketone (2×65 mL) and vacuum dry at 55° C. overnight togive the title compound (52.76 g, 97.9%); mp 197.5°-200° C.

Method D

Treat 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form II) (40.0 g, 0.0696 mol, assayed at93.6% purity, having 0.89 g water present and 35.1 g, 0.0575 mol,assayed at 88.0% purity, having 2.47 g water present) with water (8.30g; the amount calculated to bring the weight of water present to 17% ofthe anhydrous weight of 4- 4- 4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride hydrate, taking into account the water in the hydratedsalt). Add methyl ethyl ketone (approximately 500 mL) and stir untilmost of the solids dissolve. Add additional methyl ethyl ketone (700 mL)in portions over approximately 10 minutes and continue stirring for 1/2hour. Filter through a thin pad of filter aid, wash the filtercake andflask with additional methyl ethyl ketone (100 mL) and transfer to aboiling flask fitted with a thermometer, mechanical stirrer, heatingmantle, a 12-plate Oldershaw (vacuum-jacketed) distillation column and adistillation head with the capability of regulating the reflux ratio ina rough fashion, washing in with additional methyl ethyl ketone (100mL). Distill off 450 mL of solvent, cool to -15° C. and filter thesolid. Wash with methyl ethyl ketone (2×100 mL) and dry to give thetitle compound (68.3 g, 99.9%); mp 197°-199° C.

Method E

Bring methyl ethyl ketone (4 mL) to a boil and add 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride (500 mg). Decant the top layer and add methyl ethyl ketone(3 mL) to the aqueous layer. Boil the solution until the temperaturereached 79° C., reduce the volume by 25%, remove from heat and coverwith aluminum foil. Allow the solution to cool, filter the resultingcrystals and air dry to give the title compound.

EXAMPLE 26 Conversion of Form I to Form II 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate

Method A

Treat 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form I) (2.0 g) with ethanol (4 mL) and deionizedwater (20 mL). Heat at 80° C. until a solution is formed and then stirat room temperature for 23 hours. Filter the resulting slurry, wash withwater (2×10mL) and dry under vacuum at 35° C. overnight to give thetitle compound (1.88 g); mp 100°-105° C.

XRPD: Table 19

                  TABLE 19                                                        ______________________________________                                        D-Space,                                                                      Angstroms    Intensity, I/I.sub.O, %                                          ______________________________________                                        11.41        20                                                               7.98         20                                                               7.83         45                                                               6.58         45                                                               6.42         60                                                               5.66         20                                                               5.52         45                                                               5.39         30                                                               5.23         65                                                               5.14         45                                                               4.86         65                                                               4.72         100                                                              4.45         65                                                               4.40         45                                                               4.32         45                                                               4.18         45                                                               4.06         65                                                               4.02         55                                                               3.85         25                                                               3.79         75                                                               3.74         95                                                               3.61         80                                                               3.56         25                                                               3.47         65                                                               3.41         20                                                               2.74         20                                                               ______________________________________                                    

Method B

Mix water (35.5 mL), methanol (26.3 mL) and sodium chloride (2.59 g).Add 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form I) (4.77 g). Heat to reflux on a steam bathuntil dissolution and cool to -10° C. Filter the resulting solid, washwith water (2×25 mL) and vacuum dry overnight to give the title compound(4.80 g).

EXAMPLE 27 Conversion of Form II into Form III 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form III)

Place 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form II) (55.56 g, 0.0929 mol having 10%water) in a pressure bottle along with water (2.96 g) and acetone (38.1g). Seal the bottle tightly and heat to approximately 80° C. Cool toabout 50° C., filter through filter aid in a coarse sintered glassfunnel and dilute with acetone (90 g). Transfer to a 1 L flask fittedwith a mechanical stirrer, thermometer and a reflux condenser. Heat themixture to reflux and allow to cool and stir over the weekend. Cool to-15° C. and filter on a coarse sintered glass funnel, wash with ethylacetate (2×50 mL) and vacuum dry at 50° C.

Place a majority of the solid obtained (45.24 g) in a 500 mL threenecked flask fitted with a mechanical stirrer, thermometer and a refluxcondenser. Add acetone (240 mL) and water (4.82 g) and reflux themixture overnight. Allow the slurry to cool to 35° C. and place in anice water bath and cool to less then 5° C. Filter the solid off on acoarse sintered glass funnel, wash with ethyl acetate (50 mL) and vacuumdry at 50° C. for several hours to give the title compound as a whitecrystalline powder (43.83 g, 97%); mp 166.5×170.5° C. XRPD: Table 20

                  TABLE 20                                                        ______________________________________                                        D-Space,                                                                      Angstroms    Intensity, I/I.sub.O, %                                          ______________________________________                                        8.95         95                                                               4.99         20                                                               4.88         100                                                              4.75         35                                                               4.57         25                                                               4.47         25                                                               4.46         20                                                               3.67         20                                                               3.65         25                                                               ______________________________________                                    

EXAMPLE 28 Conversion of Form III into Form I 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form I)

Place 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form III) (40.0 g as an ethyl acetate wetcake-27.9 gdry basis) in a 1 L three necked flask fitted with a mechanical stirrer,thermometer and a reflux condenser. Add acetone (240 mL) and heat themixture to reflux for about 20 hours. Cool the slurry to -15° C. andisolate the solids by filtration on a coarse sintered glass frit funnel.Wash with ethyl acetate (50 mL) and vacuum dry overnight to give thetitle compound (26.1 g, 93.7%); mp 197.5°-199.5° C.

XRPD: Table 21

                  TABLE 21                                                        ______________________________________                                        D-Space,                                                                      Angstroms    Intensity, I/I.sub.O, %                                          ______________________________________                                        11.75        35                                                               7.23         35                                                               6.24         60                                                               5.89         40                                                               5.02         20                                                               4.94         30                                                               4.83         100                                                              4.44         30                                                               3.93         75                                                               3.83         20                                                               3.77         85                                                               3.71         25                                                               3.62         30                                                               3.32         25                                                               3.31         20                                                               ______________________________________                                    

EXAMPLE 29 Conversion of Form IV into Form I 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride (Form I)

Place 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride hydrate (Form IV) (54.35 g, 0.0970 mol, having 4%water present) in a pressure bottle along with water (4.16 g) andacetone (38.1 g). Seal the bottle tightly and heat to approximately 80°C. Cool to less then 60° C., filter through filter aid in a coarsesintered glass funnel and rinse the filter cake with acetone (32.4 g).Place acetone (215 g) in a 1 L three necked flask fitted with amechanical stirrer, thermometer, a reflux condenser and containing asmall amount of Form I crystals and heat to reflux. Add a portion of theacetone/water solution of 4- 4- 4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride hydrate (Form IV) (47.65 g) to the refluxing acetone overabout 10 minutes. Slowly add ethyl acetate (157.5 g) over 45 minutesthen add the remaining portion of the acetone/water solution of 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride hydrate (Form IV), rinsed in with about 20 mL of acetone.Add additional ethyl acetate (157.5 g) over 45 minutes to 1 hour,maintaining the slurry at reflux. Stir for 15 minutes, cool to -15° C.and vacuum filter the white solid on a 350 mL coarse sintered glassfunnel. Wash the solids with ethyl acetate (2×50 mL) and vacuum dryovernight to give the title compound (50.36 g, 97%); mp 198°-199.5° C.

XRPD: Table 22

                  TABLE 22                                                        ______________________________________                                        D-Space,                                                                      Angstroms    Intensity, I/I.sub.O, %                                          ______________________________________                                        14.89        20                                                               11.85        20                                                               7.30         20                                                               6.28         70                                                               5.91         25                                                               5.55         20                                                               5.05         25                                                               4.96         55                                                               4.85         100                                                              4.57         45                                                               4.45         55                                                               3.94         45                                                               3.89         20                                                               3.84         20                                                               3.78         60                                                               3.72         35                                                               3.63         20                                                               3.07         20                                                               3.04         20                                                               2.45         20                                                               ______________________________________                                    

Utilizing the procedures described in the previous examples, thecorresponding tablets and capsules may be prepared from Form I anhydrous4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride, Form III anhydrous 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride or various mixtures thereof. In addition, utilizingthe procedures described in the previous examples, the correspondingtablets and capsules may be prepared from Form II hydrated 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride, Form IV hydrated 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride or various mixtures thereof. It is readily appreciated byone of ordinary skill in the art that during the formulation process ofthe tablets and capsules described in the preceding examples,interconversion between the above described polymorphs and pseudomorphsof 4- 4- 4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,α-dimethylbenzeneacetic acidhydrochloride may occur. In addition, it is understood that theresulting tablet or capsule may contain various mixtures of Forms I, II,III and IV of 4- 4-4-(Hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride, hydrated and anhydrous.

What is claimed is:
 1. A pharmaceutical composition prepared by a wetgranulation process comprising, preparing the wet granulation wherein acompound of formula; ##STR10## wherein X is a number ranging from aboutzero to 5, and the individual optical isomers thereof, a diluent and adisintegrant are mixed with a solution of a binding agent; the wetgranulation is screened, the wet granulation is dried, and the drygranulation is screened.
 2. A pharmaceutical composition prepared by awet granulation process comprising, preparing the wet granulationwherein a compound of formula; ##STR11## wherein X is a number rangingfrom about zero to 5, and the individual optical isomers thereof, adiluent and a disintegrant are mixed with a solution of a binding agent;the wet granulation is screened, the wet granulation is dried and thedry granulation is combined with a lubricant.
 3. A pharmaceuticalcomposition in solid unit dosage form prepared by a process comprisingblending together a compound of the formula; ##STR12## wherein X is anumber ranging from about zero to 5, and the individual optical isomersthereof, with microcrystalline cellulose, calcium carbonate andpregelatinized starch; adding a solution of gelatin in water withmixing; drying the granulated mixture; adding additionalmicrocrystalline cellulose and sodium starch glycolate with blending;and adding magnesium stearate with blending.
 4. A pharmaceuticalcomposition in solid unit dosage form according to claim 3 wherein thefinal mixture is pressed into tablets.
 5. A pharmaceutical compositionin solid unit dosage form according to claim 3 wherein themicrocrystalline cellulose, calcium carbonate, pregelatinized starch,gelatin, sodium starch glycolate and magnesium stearate are combined intotal amounts of about 34.9%, 15.6%, 29.4%, 3.3%, 5.6% and 0.5%,respectively, by weight of the composition.
 6. A pharmaceuticalcomposition in solid unit dosage form prepared by a process comprisingblending together a compound of the formula; ##STR13## wherein X is anumber ranging from about zero to 5, and the individual optical isomersthereof, with microcrystalline cellulose, calcium carbonate andpregelatinized starch; adding water with mixing; drying the granulatedmixture; adding additional microcrystalline cellulose and sodium starchglycolate, with blending; and adding magnesium stearate with blending.7. A pharmaceutical composition in solid unit dosage form according toclaim 6 wherein the final mixture is pressed into tablets.
 8. Apharmaceutical composition in solid unit dosage form according to claim6 wherein the microcrystalline cellulose, calcium carbonate,pregelatinized starch, sodium starch glycolate and magnesium stearateare combined in total amounts of about 336.5%, 15.6%, 31.0%, 5.6% and0.5%, respectively, by weight of the composition.
 9. A pharmaceuticalcomposition in solid unit dosage form, comprising;a) a therapeuticallyeffective amount of a piperidinoalkanol compound of the formula;##STR14## wherein X is a number ranging from about zero to 5, and theindividual optical isomers thereof; and b) inert ingredients, comprisingmicrocrystalline cellulose, pregelatinized starch, gelatin, magnesiumstearate, calcium carbonate and sodium starch glycolate.
 10. Thepharmaceutical composition in solid unit dosage form according to claim9 wherein microcrystalline cellulose, pregelatinized starch, gelatin,magnesium stearate, calcium carbonate and sodium starch glycolate arepresent in amounts of about 20% to about 85%, 5% to about 50%, 1% toabout 15%, 0.05% to about 3%, 5% to about 50% and 1% to about 15%,respectively, by weight of the composition.
 11. The pharmaceuticalcomposition in solid unit dosage form according to claim 9 whereinmicrocrystalline cellulose, pregelatinized starch, gelatin, magnesiumstearate, calcium carbonate and sodium starch glycolate are present inamounts of about 34.9%, 29.4%, 3.3%, 0.5%, 15.6%, 5.6%, respectively, byweight of the composition.
 12. A pharmaceutical composition in solidunit dosage form, comprising;a) a therapeutically effective amount of apiperidinoalkanol compound of the formula; ##STR15## wherein X is anumber ranging from about zero to 5, and the individual optical isomersthereof; and b) inert ingredients comprising microcrystalline cellulose,pregelatinized starch, magnesium stearate, calcium carbonate and sodiumstarch glycolate.
 13. The pharmaceutical composition in solid unitdosage form according to claim 12 wherein microcrystalline cellulose,pregelatinized starch, magnesium stearate, calcium carbonate and sodiumstarch glycolate are present in amounts of about 20% to about 85%, 5% toabout 50%, 0.05% to about 3%, 5% to about 50% and 1% to about 15%,respectively, by weight of the composition.
 14. The pharmaceuticalcomposition in solid unit dosage form according to claim 12 whereinmicrocrystalline cellulose, pregelatinized starch, magnesium stearate,calcium carbonate and sodium starch glycolate are present in amounts ofabout 36.5%, 31.0%, 0.5%, 15.6%, and 5.6%, respectively, by weight ofthe composition.
 15. The pharmaceutical composition in solid unit dosageform according to claim 12 wherein microcrystalline cellulose,pregelatinized starch, magnesium stearate, calcium carbonate and sodiumstarch glycolate are present in amounts of about 21.1%, 30.0%, 0.75%,15.6%, and 10.0%, respectively, by weight of the composition.
 16. Thepharmaceutical composition in solid unit dosage form as in either claims11, 14 or 15 wherein said piperidinoalkanol compound is 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride.
 17. The pharmaceutical composition in solid unitdosage form according to claim 16 wherein 4- 4-4-(hydroxydiphenylmethyl)-1-piperidinyl!-1-hydroxybutyl!-α,.alpha.-dimethylbenzeneaceticacid hydrochloride is present in an amount of about 5 mg to about 180mg.
 18. A pharmaceutical composition in solid form whereinmicrocrystalline cellulose, pregelatinized starch, magnesium stearate,calcium carbonate and sodium starch glycolate are present in amounts ofabout 21.1%, 30.0%, 0.75%, 15.6%, and 10.0%, respectively, by weight ofthe composition wherein the final mixture is pressed into a tablet fromwhich the quantity of compound of the formula; ##STR16## wherein X is anumber ranging from about zero to 5, and the individual optical isomersthereof, dissolved in 45 minutes, is not less than 75% of label in0.001N aqueous hydrochloric acid at about 37° C. and about 50 rpm whenmeasured using USP Apparatus 2.